Benzyloxycarbonylglycyl-L-prolyl-L-leucylglycine

Description

Benzyloxycarbonylglycyl-L-prolyl-L-leucylglycine
Catalog number: MDP0058
CAS Number: 113865-89-7
Sequence: Benzyloxycarbonylglycyl-L-prolyl-L-leucylglycine
Amount: 10 mg
Molecular Weight: 476.4 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20 °C
WARNING: For in vitro Research Use Only. NOT for use on humans or animals.
Grade: Biotechnology grade. All products are highly pure.

References:
1: Friedman TC, Orlowski M, Wilk S. Prolyl endopeptidase: inhibition in vivo by N-benzyloxycarbonyl-prolyl-prolinal J Neurochem. 1984 Jan;42(1):237-41.
2: Wolf DH, Ehmann C. Carboxypeptidase S- and carboxypeptidase Y-deficient mutants of Saccharomyces cerevisiae J Bacteriol. 1981 Aug;147(2):418-26.
3: Steinauer R, Chen FM, Benoiton NL. Studies on racemization associated with the use of benzotriazol-1-yl-tris (dimethylamino)phosphonium hexafluorophosphate (BOP) Int J Pept Protein Res. 1989 Oct;34(4):295-8.
4: Benoiton NL, Kuroda K. Studies on racemization during couplings using a series of model tripeptides involving activated residues with unfunctionalized side chains Int J Pept Protein Res. 1981 Feb;17(2):197-204.
5: Alecio MR, Dann ML, Lowe G. The specificity of the S1′ subsite of papain Biochem J. 1974 Aug;141(2):495-501.
6: Seber JF, Toomey TP, Powell JT, Brew K, Awad WM Jr. Proteolytic enzymes of the K-1 strain of Streptomyces griseus obtained from a commercial preparation (Pronase). Purification and characterization of the carboxypeptidase J Biol Chem. 1976 Jan 10;251(1):204-8.
7: Gray CJ, Barker SA, Dhariwal MS, Sullivan JM. Assay of the high-alkaline proteinase from alkalophilic bacillus PB92 using a chromogenic tripeptide substrate Biotechnol Bioeng. 1985 Dec;27(12):1717-20.
8: Whitaker JR. Kinetics of the carboxypeptidase A-catalyzed hydrolysis of benzyloxycarbonylglycyl-L-phenylalanine Biochem Biophys Res Commun. 1966 Jan 4;22(1):6-12.
9: Leytus SP, Patterson WL, Mangel WF. New class of sensitive and selective fluorogenic substrates for serine proteinases. Amino acid and dipeptide derivatives of rhodamine Biochem J. 1983 Nov 1;215(2):253-60.
10: Tomatis R, Ferroni R, Guarneri M, Benassi CA. [Use of oximinoiminopyrrazoline esters in the synthesis of solids phase peptides: synthesis of bradykinin] Farmaco Sci. 1976 Jan;31(1):70-9.

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